4.5 Article

Near-Infrared Optical Spectroscopy In Vivo Distinguishes Subjects with Alzheimer's Disease from Age-Matched Controls

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 82, Issue 2, Pages 791-802

Publisher

IOS PRESS
DOI: 10.3233/JAD-201021

Keywords

Alzheimer's disease; cognitive dysfunction; data analysis; mild cognitive impairment; near-infrared spectroscopy

Categories

Funding

  1. U.S. Department ofVeterans Affairs, Clinical Sciences Research and Development Service [I01 CX000827]
  2. U.S. Department of Health and Human Services, National Institutes of Health, National Institute on Aging [P30 AG013846]
  3. Headwall Photonics, Inc.

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The study aimed to determine whether NIR spectroscopy can distinguish Alzheimer's disease patients from controls in clinical applications and show the potential of NIR as a clinical screen and monitor of therapeutic efficacy. The results indicate that two regions around 860 and 895 nm can completely separate AD patients from controls and differentiate MCI subjects according to the degree of impairment.
Background: Medical imaging methods such as PET and MRI aid clinical assessment of Alzheimer's disease (AD). Less expensive, less technically demanding, and more widely deployable technologies are needed to expand objective screening for diagnosis, treatment, and research. We previously reported brain tissue near-infrared optical spectroscopy (NIR) in vitro indicating the potential to meet this need. Objective: To determine whether completely non-invasive, clinical, NIR in vivo can distinguish AD patients from age-matched controls and to show the potential of NIR as a clinical screen and monitor of therapeutic efficacy. Methods: NIR spectra were acquired in vivo. Three groups were studied: autopsy-confirmed AD, control and mild cognitive impairment (MCI). A feature selection approach using the first derivative of the intensity normalized spectra was used to discover spectral regions that best distinguished AD-alone (i.e., without other significant neuropathology) from controls. The approach was then applied to other autopsy-confirmed AD cases and to clinically diagnosed MCI cases. Results: Two regions about 860 and 895 nm completely separate AD patients from controls and differentiate MCI subjects according to the degree of impairment. The 895 nm feature is more important in separating MCI subjects from controls (ratio-of-weights: 1.3); the 860 nm feature is more important for distinguishing MCI from AD (ratio-of-weights: 8.2). Conclusion: These results form a proof of the concept that near-infrared spectroscopy can detect and classify diseased and normal human brain in vivo. A clinical trial is needed to determine whether the two features can track disease progression and monitor potential therapeutic interventions.

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